Expression profile and N6-methyadenosine modification of circular RNA analysis in MAFLD.

IF 2.5 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY BMC Gastroenterology Pub Date : 2025-03-11 DOI:10.1186/s12876-025-03722-4
Mengyao Zheng, Dongyun Cun, Haiyu He, Xuancheng Xie, Hongtao Lei, Wen Fu, Wenlin Tai, Jinhui Yang
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Abstract

Background: To analyze the expression patterns of circRNAs in metabolic associated fatty liver disease (MAFLD) and the regulation of m6A methylation on those circRNAs.

Methods: The expression profile of CircRNA in MAFLD and normal control liver tissues was analyzed by microarray. Predict the potential m6A sites of the differentially expression circRNAs (DECs) via the SRAMP website. The biological functions and molecular interactions of DECs were analyzed by GO and KEGG analyses. The selected DECs were verified by MeRIP-qPCR and RT-qPCR.

Results: There were 59 DECs in MAFLD liver tissues compared with normal control liver tissues. We found that m6A sites with high or very high confidence were present in 39 of these DECs. Four randomly selected DECs were validated by RT-qPCR, hsa-MLIP_0004, hsa-CHD2_0084 and hsa-FOXP1_0001 matched well with the microarray results. m6A qualification of them were conducted by MeRIP-qPCR, the m6A methylation levels are significantly different between the MAFLD and NC groups.

Conclusion: In MAFLD, the dysregulated expression of circRNAs may be influenced by m6A modifications. This study provides preliminary evidence suggesting that m6A-mediated regulation of circRNAs could play a role in the progression of MAFLD, laying the foundation for exploring the epigenetic regulation of circRNAs in MAFLD and offering potential avenues for future diagnostic and therapeutic strategies.

Trial registration: Not applicable.

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环状RNA的表达谱及n6 -甲基腺苷修饰分析。
背景:分析代谢性脂肪性肝病(MAFLD)中circrna的表达模式以及m6A甲基化对这些circrna的调控。方法:采用芯片分析CircRNA在MAFLD和正常对照肝组织中的表达谱。通过SRAMP网站预测差异表达环状rna (DECs)的潜在m6A位点。采用GO和KEGG分析了DECs的生物学功能和分子相互作用。选取的DECs经MeRIP-qPCR和RT-qPCR验证。结果:与正常对照肝组织相比,MAFLD肝组织中存在59个DECs。我们发现在39个DECs中存在高置信度或非常高置信度的m6A位点。随机选择4个DECs进行RT-qPCR验证,hsa-MLIP_0004、hsa-CHD2_0084和hsa-FOXP1_0001与芯片结果吻合良好。通过MeRIP-qPCR对m6A进行鉴定,m6A甲基化水平在MAFLD组和NC组之间存在显著差异。结论:在MAFLD中,circrna的表达失调可能受到m6A修饰的影响。本研究提供了初步证据,表明m6a介导的circRNAs调控可能在MAFLD的进展中发挥作用,为探索MAFLD中circRNAs的表观遗传调控奠定了基础,并为未来的诊断和治疗策略提供了潜在的途径。试验注册:不适用。
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来源期刊
BMC Gastroenterology
BMC Gastroenterology 医学-胃肠肝病学
CiteScore
4.20
自引率
0.00%
发文量
465
审稿时长
6 months
期刊介绍: BMC Gastroenterology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of gastrointestinal and hepatobiliary disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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